- Trials with a EudraCT protocol (55)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (2)
55 result(s) found for: Zyprexa AND olanzapine.
Displaying page 3 of 3.
EudraCT Number: 2013-005399-16 | Sponsor Protocol Number: ROAC2014 | Start Date*: 2014-08-05 | |||||||||||
Sponsor Name:Dr. Benedicto Crespo. Servicio Psiquiatría. Hospital Universitario Marqués de Valdecilla/IDIVAL | |||||||||||||
Full Title: Randomized, flexible-dose, open-label comparison to investigate the effectivenes of second generation antipsychotics in first episode psychosis patients. | |||||||||||||
Medical condition: FIRST EPISODE DRUG-NAÏVE OF PSYCHOSIS (SCHIZOPHRENIA SPECTRUM DISORDERS) | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-000479-11 | Sponsor Protocol Number: 12396A | Start Date*: 2008-07-21 | ||||||||||||||||||||||||||
Sponsor Name:H. Lundbeck A/S | ||||||||||||||||||||||||||||
Full Title: A randomised, double-blind, parallel-group, active-controlled, flexible dose study exploring the efficacy and safety of 12 weeks treatment with Lu 31-130 in patients with schizophrenia | ||||||||||||||||||||||||||||
Medical condition: Lu 31-130 is under development by H. Lundbeck A/S as an antipsychotic in the treatment of schizophrenia | ||||||||||||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: CZ (Completed) FR (Completed) ES (Completed) | ||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2009-012031-15 | Sponsor Protocol Number: 01KG0910 | Start Date*: 2009-11-19 | |||||||||||||||||||||
Sponsor Name:Technische Universitaet Muenchen, vertreten durch das Klinikum rechts der Isar | |||||||||||||||||||||||
Full Title: The switch study - efficacy of early antipsychotic switch versus maintenance in patients with schizophrenia poorly responding to two weeks of antipsychotic treatment | |||||||||||||||||||||||
Medical condition: Patients with a diagnosis of schizophrenia , schizophreniform disorder or schizoaffective disorder according to DSM-IV TR criteria; experiencing an acute episode of their illness | |||||||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: DE (Completed) RO (Completed) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2008-008366-13 | Sponsor Protocol Number: 3.0edition | Start Date*: 2009-03-17 | |||||||||||||||||||||||||||||||
Sponsor Name:Unit for Psychiatric Research | |||||||||||||||||||||||||||||||||
Full Title: Comparison of the effects of Sertindole and Olanzapine on Cognition | |||||||||||||||||||||||||||||||||
Medical condition: Cognitive deficits in patients with schizophrenia | |||||||||||||||||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||||||||||||||||||||||
Trial protocol: DK (Prematurely Ended) SE (Completed) | |||||||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-004897-26 | Sponsor Protocol Number: Lu-11829A | Start Date*: 2008-05-23 | |||||||||||
Sponsor Name:King's College London [...] | |||||||||||||
Full Title: Memantine for the Long Term Management of Neuropsychiatric Symptoms in Alzheimer's disease - MAIN-AD | |||||||||||||
Medical condition: Alzheimer's disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-017853-36 | Sponsor Protocol Number: H8Y-MC-HBBO | Start Date*: 2010-09-07 | |||||||||||
Sponsor Name:Eli Lilly and Company | |||||||||||||
Full Title: A Long-Term, Open-Label, Multicenter Study of LY2140023 Compared to Atypical Antipsychotic Standard of Care in Patients with DSM-IV-TR Schizophrenia | |||||||||||||
Medical condition: Schizophrenia | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-003820-40 | Sponsor Protocol Number: D1050231 | Start Date*: 2008-03-17 | |||||||||||
Sponsor Name:Dainippon Sumitomo Pharma America, Inc. | |||||||||||||
Full Title: A Phase 3 Randomized, Placebo- and Active Comparator-Controlled Clinical Trial to Study the Safety and Efficacy of Two Doses of Lurasidone HCl in Acutely Psychotic Patients with Schizophrenia | |||||||||||||
Medical condition: Schizophrenia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: LT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-018665-30 | Sponsor Protocol Number: KKSH-079 | Start Date*: 2010-06-30 | ||||||||||||||||
Sponsor Name:Martin-Luther University Halle-Wittenberg | ||||||||||||||||||
Full Title: COMFORT-study Comparison of Olanzapin and Metoclopramide For treatment Of bReakThrough emesis | ||||||||||||||||||
Medical condition: Patienten, die trotz maximaler Standardantiemese mit Granisetron, Dexamethason und Aprepitant unter chemotherapie-induzierter Übelkeit und Erbrechen leiden. | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Prematurely Ended) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2010-021984-33 | Sponsor Protocol Number: WN25333 | Start Date*: 2011-05-02 | |||||||||||||||||||||
Sponsor Name:F. Hoffmann-La Roche Ltd | |||||||||||||||||||||||
Full Title: A phase II/III, multi-center, randomized, 4-week, double-blind, parallel group, placebo and active-controlled trial of the safety and efficacy of RO4917838 vs. placebo in patients with an acute exa... | |||||||||||||||||||||||
Medical condition: Acute Symptoms of Schizophrenia | |||||||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: SK (Completed) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2004-000113-18 | Sponsor Protocol Number: CLIC477D2302 | Start Date*: 2004-09-23 |
Sponsor Name:Novartis Farmacéutica, S.A. | ||
Full Title: A randomized, double-blind, placebo-controlled, multicenter study to evaluate the efficacy, safety and tolerability of licarbazepine 750-2500 mg/d combined with risperidone in the treatment of mani... | ||
Medical condition: Bipolar I disorder, manic and mixed episodes | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Completed) HU (Completed) FI (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2007-000800-34 | Sponsor Protocol Number: H8Y-MC-HBBI | Start Date*: 2007-08-14 | |||||||||||||||||||||||||||||||
Sponsor Name:Eli Lilly and Company Ltd. | |||||||||||||||||||||||||||||||||
Full Title: A Multi-center, Inpatient, Phase 2, Double-blind, Placebo-controlled Dose Ranging Study of LY2140023 in Patients with DSM-IV Schizophrenia. | |||||||||||||||||||||||||||||||||
Medical condition: Patients must have a diagnosis of Schizophrenia as defined in Diagnostic and Statistical Manual of Mental Disorders, Fourth Edition (DSM-IV) (Disorganized, 295.10; Catatonic, 295.20; Paranoid, 295.... | |||||||||||||||||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||||||||||||||||||||||
Trial protocol: DE (Completed) PT (Completed) AT (Completed) | |||||||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2009-016245-26 | Sponsor Protocol Number: H8Y-MC-HBCO | Start Date*: 2010-02-02 | |||||||||||
Sponsor Name:Lilly S.A | |||||||||||||
Full Title: Estudio de Fase 2, de 17 Semanas, Multicéntrico, Aleatorizado y Doble Ciego, Sobre la Eficacia de LY2140023 Combinado con Tratamiento Clínico Habitual Comparado con Placebo Combinado con Tratamient... | |||||||||||||
Medical condition: Esquizofrenia | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-004881-33 | Sponsor Protocol Number: 73-05-3832-397285-12 | Start Date*: 2017-02-28 |
Sponsor Name:Universitätsklinikum Würzburg | ||
Full Title: Pharmacovigilance in children and adolescents: clinical trial protocol, subproject 1: Large Simple Trial, IIIb on the (off-label-) use of antidepressants and antipsychotics | ||
Medical condition: therapeutic use in clinical practise | ||
Disease: | ||
Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |
Trial protocol: DE (Completed) AT (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2015-003284-11 | Sponsor Protocol Number: 16159B | Start Date*: 2016-09-22 | |||||||||||
Sponsor Name:H. Lundbeck A/S | |||||||||||||
Full Title: Interventional, open-label, flexible-dose, long-term safety study of Lu AF35700 in adult patients with schizophrenia | |||||||||||||
Medical condition: Treatment-resistant schizophrenia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) CZ (Completed) SK (Completed) EE (Completed) FI (Completed) BG (Completed) PL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-004327-13 | Sponsor Protocol Number: H8Y-MC-HBBV | Start Date*: 2012-02-06 | |||||||||||
Sponsor Name:Eli Lilly and Company | |||||||||||||
Full Title: Long-Term Open-Label Safety Study of Pomaglumetad Methionil in Patients with Schizophrenia | |||||||||||||
Medical condition: Schizophrenia | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: GR (Prematurely Ended) DE (Completed) ES (Prematurely Ended) BE (Prematurely Ended) AT (Prematurely Ended) SE (Prematurely Ended) | |||||||||||||
Trial results: View results |
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